Skip to main content
. 2002 Jan 21;2002(1):CD002123. doi: 10.1002/14651858.CD002123

Santiesteban 1985.

Methods Participants blinded 
 Parallel design 
 8 women randomised and analysed
Participants Inclusion: dysmenorrhoea 
 Exclusion: any medication 
 Age: average 22 years 
 Location: USA
Interventions 1. Low‐frequency TENS ‐ 5 Hz pulse rate, 250 μsec, pulse duration/intensity to patients tolerance 
 2. Sham (mock) TENS ‐ no intensity administered 
 Duration: 30 min 
 Location: Spleen 6, Gallbladder 34 (on legs)
Outcomes Pain scale 1‐5 measured pre, post, 4 hrs, 24 hrs, 30 days 
 Abdominal pain 
 Back pain
Notes No difference between the experimental and control group for pretreatment abdominal pain, however there was some difference for pretreatment back pain with the control group having a higher average pain rating